Employment Type : Full-Time
Walker Cole International is searching for a QA Validation Specialist to join an exciting Global Pharmaceutical company based in the South-West of the UK. As the QA Validation Specialist, you will be responsible for performing a range of validation activities at the site. Key Responsibilities as the QA Validation Specialist: Performing validation activities at the site including Facility, equipment, and process validation. Working with the team ...
Employment Type : Full-Time
The purpose of this role of Quality Validation Specialist is to ensure product and system quality. Your will be evaluating engineering systems based on safety and performance standards and analyse results and update activity logs Design or plan validation protocols and other documentation for equipment, processes or products meeting internal and external safety and quality requirements. Conduct validation or qualification tests for new or existi...
Employment Type : Full-Time
Quality Assurance Engineer up to 2 Year Contract Birmingham Competitive Rates *** Due to the nature of the role & the industry you are working in, you will be required to achieve UK BPSS & SC clearance *** We are looking for a Quality Specialist to support the Audit Programme. Ideally, you will have come from a Production or Manufacturing background (not maintenance) with strong Quality, Audit and Investigation experience as you will be ...
Employment Type : Full-Time
Summary Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra. Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide. Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2000 colleagues globally. Fro...
Employment Type : Full-Time
Dr. Martens is a globally recognisable and culturally influential British brand, with over 60 years of rich heritage. As brand custodians, we are lucky to work for a dynamic, thriving, and ethical business, with people from diverse backgrounds, who bring their true selves to work, and where anyone can grow their career. We are guided by three core values that are at the heart of everything we do: be yourself , act courageously , and show you car...
Employment Type : Full-Time
Walker Cole International is searching for a Serialisation Specialist to join an exciting Global Pharmaceutical company based in the Greater London Area. As the Serialisation Specialist, you will get the chance to ensure that the serialisation processes are robust and efficient, and compliant with the Falsified Medicines Directive (FMD). Key Responsibilities as the Serialisation Specialist: Ensure the correct functioning and operation of the ser...
Employment Type : Full-Time
An opportunity has arisen for a Quality Control Specialist to join the growing team of scientists based in the southwest area. The successful individual has a working knowledge of Quality, GMP and GLP practices. The Quality Control Specialist will play a vital role in ensuring adherence to quality standards, GMP (Good Manufacturing Practice), and GLP (Good Laboratory Practice) guidelines. The successful candidate will be responsible for coordina...
Employment Type : Full-Time
Mechanical Engineer - Verification & Validation Biotech - Cambridge A growing Biotech company, based in Cambridge, are currently looking for a Mechanical Engineer who help with the company's successful Verification & Validation activities, from a mechanical engineering viewpoint. After around six months, the Verification & Validation duties will reduce, allowing you to focus your work into Mechanical Engineering duties. We are lookin...
Employment Type : Full-Time
Role Title Quality Control Officer Fixed Term Contact 6 Month Initial Term Haverhill 35,000 Benefits Role Profile Ensure the PQMS is maintained in a state of control across all locations. Ensure activities performed by the Quality department are performed in accordance with GMP, GDP, IOS 9001 and ISO 13485 requirements. To control and preparation of PQMS documents including SOPs, validation, Complaints, change controls, CAPAs, and deviations. To...
Employment Type : Full-Time
Your experience of systems engineering (specifically systems requirements, design and integration) will help you to deliver innovative solutions as a Systems Engineer. As a Systems Engineering specialist, you will be responsible for leading all technical aspects of engineering projects. You will have the opportunity to work for a company passionate about inertial navigation and GNSS and how they can help their customers through integration of th...